Lu CS - Search Results

1

Identification of a novel intronic variant in COL4A2 gene associated with fetal severe cerebral encephalomalacia and subdural hemorrhage.

Sun RY, Xu Y, Huang QQ, Hu SS, Xu HZ, Luo YZ, Zhu T, Sun JH, Gong YJ, Zhu MM, Wang HW, Pan JY, Lu CS, Wang D. Sun RY, et al. Among authors: lu cs. BMC Med Genomics. 2024 Sep 30;17(1):238. doi: 10.1186/s12920-024-02012-4. BMC Med Genomics. 2024. PMID: 39350129 Free PMC article.

2

CircNr1h4 regulates the pathological process of renal injury in salt-sensitive hypertensive mice by targeting miR-155-5p.

Lu C, Chen B, Chen C, Li H, Wang D, Tan Y, Weng H. Lu C, et al. J Cell Mol Med. 2020 Jan;24(2):1700-1712. doi: 10.1111/jcmm.14863. Epub 2019 Nov 28. J Cell Mol Med. 2020. PMID: 31782248 Free PMC article.

3

Neonatal Ureaplasma parvum meningitis: a case report and literature review.

Wang Q, Wang K, Zhang Y, Lu C, Yan Y, Huang X, Zhou J, Chen L, Wang D. Wang Q, et al. Transl Pediatr. 2020 Apr;9(2):174-179. doi: 10.21037/tp.2020.02.04. Transl Pediatr. 2020. PMID: 32477918 Free PMC article.

4

AICAR, an AMP-Activated Protein Kinase Activator, Ameliorates Acute Pancreatitis-Associated Liver Injury Partially Through Nrf2-Mediated Antioxidant Effects and Inhibition of NLRP3 Inflammasome Activation.

Kong L, Zhang H, Lu C, Shi K, Huang H, Zheng Y, Wang Y, Wang D, Wang H, Huang W. Kong L, et al. Front Pharmacol. 2021 Aug 31;12:724514. doi: 10.3389/fphar.2021.724514. eCollection 2021. Front Pharmacol. 2021. PMID: 34531748 Free PMC article.

5

Fibroblast growth factor 21 attenuates salt-sensitive hypertension-induced nephropathy through anti-inflammation and anti-oxidation mechanism.

Weng HC, Lu XY, Xu YP, Wang YH, Wang D, Feng YL, Chi Z, Yan XQ, Lu CS, Wang HW. Weng HC, et al. Among authors: lu cs, lu xy. Mol Med. 2021 Nov 13;27(1):147. doi: 10.1186/s10020-021-00408-x. Mol Med. 2021. PMID: 34773993 Free PMC article.

6

Novel compound heterozygous SUCLG1 variants may contribute to mitochondria DNA depletion syndrome-9.

Chen YM, Chen W, Xu Y, Lu CS, Zhu MM, Sun RY, Wang Y, Chen Y, Shi J, Wang D. Chen YM, et al. Among authors: lu cs. Mol Genet Genomic Med. 2022 Sep;10(9):e2010. doi: 10.1002/mgg3.2010. Epub 2022 Jun 28. Mol Genet Genomic Med. 2022. PMID: 35762302 Free PMC article.

7

[Analysis of phenotype and genetic variant in a family with Shprintzen-Goldberg syndrome].

Shi J, Sun J, Chen Y, Zhu M, Wang Q, Lu C, Wang D. Shi J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Jul 10;39(7):703-707. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35810425 Chinese.

8

A novel chromosome 2q24.3-q32.1 microdeletion in a fetus with multiple malformations.

Zhu M, Wang Y, Guan L, Lu C, Sun R, Chen Y, Shi J, Zhu Y, Wang D. Zhu M, et al. J Clin Lab Anal. 2022 Aug;36(8):e24602. doi: 10.1002/jcla.24602. Epub 2022 Jul 12. J Clin Lab Anal. 2022. PMID: 35819063 Free PMC article.

9

[Analysis of PROC gene variant in a Chinese pedigree affected with hereditary protein C deficiency].

Chen Y, Shi J, Huang X, Sheng A, Lu C, Zhu M, Wang Q, Wang M, Wang D. Chen Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Nov 10;39(11):1233-1237. doi: 10.3760/cma.j.cn511374-20210809-00661. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 36317209 Chinese.

10

[Clinical phenotype and genetic analysis of a child with 3p26.3p25.3 deletion].

Shi J, Chen S, Lu A, Liang Y, Wang Q, Lu C, Wang D. Shi J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Feb 10;40(2):234-237. doi: 10.3760/cma.j.cn511393-20220412-00247. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 36709948 Chinese.

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